Detalhe da pesquisa
1.
Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.
Am J Med Genet A
; 188(8): 2376-2388, 2022 08.
Artigo
Inglês
| MEDLINE | ID: mdl-35716026
2.
Integrative analysis of noncoding mutations identifies the druggable genome in preterm birth.
Sci Adv
; 10(3): eadk1057, 2024 Jan 19.
Artigo
Inglês
| MEDLINE | ID: mdl-38241369
3.
Systems analysis of de novo mutations in congenital heart diseases identified a protein network in the hypoplastic left heart syndrome.
Cell Syst
; 13(11): 895-910.e4, 2022 11 16.
Artigo
Inglês
| MEDLINE | ID: mdl-36167075